Is Engrailed-2 (EN2) a truly promising biomarker in prostate cancer detection?
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
- Keywords
- EN2, Prostate cancer, biomarkers, engrailed-2, urinary,
- MeSH
- Urinalysis MeSH
- Biopsy MeSH
- Adult MeSH
- Enzyme-Linked Immunosorbent Assay MeSH
- Homeodomain Proteins urine MeSH
- Kallikreins blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Biomarkers, Tumor blood urine MeSH
- Prostatic Neoplasms blood diagnosis pathology urine MeSH
- Predictive Value of Tests MeSH
- Prostate-Specific Antigen blood MeSH
- Nerve Tissue Proteins urine MeSH
- Aged MeSH
- Neoplasm Staging MeSH
- Case-Control Studies MeSH
- Neoplasm Grading MeSH
- Tumor Burden MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- engrailed 2 protein MeSH Browser
- Homeodomain Proteins MeSH
- Kallikreins MeSH
- KLK3 protein, human MeSH Browser
- Biomarkers, Tumor MeSH
- Prostate-Specific Antigen MeSH
- Nerve Tissue Proteins MeSH
Purpose: Prostate-specific antigen (PSA) is a sensitive but unspecific marker for prostate cancer (PC) detection, which may result in harms including overdiagnosis and overtreatment. Therefore, the development of new markers is of absolute value. The urinary level of engrailed-2 (EN2) protein has been recently suggested as a promising PC biomarker, correlating with tumour volume and stage. This study evaluated EN2 and its potential use in clinical practice.Materials and methods: Urinary EN2 was assessed by different commercially available enzyme-linked immunosorbent assay kits. The study sample included 90 patients with clinically localized PC compared to 30 healthy controls, and a group of 40 patients indicated for prostate biopsy due to an elevated PSA level where both pre- and post-digital rectal examination urine samples were collected.Results: No statistical difference between the patient group and the control group was obtained in all measured variables. There was no significant correlation between urinary EN2 and serum PSA, tumour staging and grading. Attentive DRE did not lead to significant changes of urinary EN2 or impact on its predictive power.Conclusions: Our results show that EN2 as a PC biomarker brings no additional value to the current use of PSA in clinical practice.
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